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Best matches for "trisomy 22":

Two trisomy 22 live births in one hospital in 15 months: is it as rare as we thought? Naicker T et al. Fetal Pediatr Pathol. (2014)

Co-occurrence of non-mosaic trisomy 22 and inherited balanced t(4;6)(q33;q23.3) in a liveborn female: case report and review of the literature. Kehinde FI et al. Am J Med Genet A. (2014)

[Trisomy 22 syndrome: a case report]. Yan JX et al. Zhongguo Dang Dai Er Ke Za Zhi. (2015)

Search results

Items: 1 to 20 of 277

1.

Chromosomal karyotype in chorionic villi of recurrent spontaneous abortion patients.

Du Y, Chen L, Lin J, Zhu J, Zhang N, Qiu X, Li D, Wang L.

Biosci Trends. 2018;12(1):32-39. doi: 10.5582/bst.2017.01296.

2.

SNP-array lesions in core binding factor acute myeloid leukemia.

Duployez N, Boudry-Labis E, Roumier C, Boissel N, Petit A, Geffroy S, Helevaut N, Celli-Lebras K, Terré C, Fenneteau O, Cuccuini W, Luquet I, Lapillonne H, Lacombe C, Cornillet P, Ifrah N, Dombret H, Leverger G, Jourdan E, Preudhomme C.

Oncotarget. 2018 Jan 8;9(5):6478-6489. doi: 10.18632/oncotarget.24031. eCollection 2018 Jan 19.

3.

Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism.

Chen CP, Tsai C, Lin MH, Chern SR, Chen SW, Lai ST, Chen WL, Pan CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Oct;56(5):691-693. doi: 10.1016/j.tjog.2017.09.001.

4.

Development of a Chromosomal Microarray Test for the Detection of Abnormalities in Formalin-Fixed, Paraffin-Embedded Products of Conception Specimens.

Gliem TJ, Aypar U.

J Mol Diagn. 2017 Nov;19(6):843-847. doi: 10.1016/j.jmoldx.2017.07.001. Epub 2017 Aug 12.

PMID:
28807814
5.

[Chorionic villus cell culture and karyotype analysis in 1 983 cases of spontaneous miscarriage].

Yuan SM, Liao C, Li DZ, Huang JZ, Hu SY, Ke M, Zhong HZ, Yi CX.

Zhonghua Fu Chan Ke Za Zhi. 2017 Jul 25;52(7):461-466. doi: 10.3760/cma.j.issn.0529-567X.2017.07.006. Chinese.

PMID:
28797153
6.

Effect of maternal age on spontaneous abortion during the first trimester in Northeast China.

Dai R, Li L, Zhu H, Geng D, Deng S, Liu R.

J Matern Fetal Neonatal Med. 2018 Jul;31(14):1824-1829. doi: 10.1080/14767058.2017.1330330. Epub 2017 May 31.

PMID:
28502197
7.

Chimpanzee Down syndrome: a case study of trisomy 22 in a captive chimpanzee.

Hirata S, Hirai H, Nogami E, Morimura N, Udono T.

Primates. 2017 Apr;58(2):267-273. doi: 10.1007/s10329-017-0597-8. Epub 2017 Feb 21.

PMID:
28220267
8.

Detection of aneuploidies in spontaneous abortions by quantitative fluorescent PCR with short tandem repeat markers: a retrospective study.

Coelho FF, Marques FK, Gonçalves MS, Almeida VC, Mateo EC, Ferreira AC.

Genet Mol Res. 2016 Sep 23;15(3). doi: 10.4238/gmr.15038617.

PMID:
27706771
9.

Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability.

Naoufal R, Legendre M, Couet D, Gilbert-Dussardier B, Kitzis A, Bilan F, Harbuz R.

Eur J Med Genet. 2016 Sep;59(9):483-7. doi: 10.1016/j.ejmg.2016.07.001. Epub 2016 Jul 21.

PMID:
27452446
10.

Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report.

Vahidi Mehrjardi MY, Dehghan Tezerjani M, Nori-Shadkam M, Kalantar SM, Dehghani M.

Iran J Public Health. 2016 Mar;45(3):376-80.

11.

[Detection of chromosome aneuploidies in spontaneous abortion villus samples by quantitative fluorescence PCR].

Wu Z, Liu N, Zhao Y, Zhao Z, Kong X.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Apr;33(2):227-30. doi: 10.3760/cma.j.issn.1003-9406.2016.02.022. Chinese.

PMID:
27060322
12.

[Refractory primary myeloid sarcoma of the breast with MLL-AF9 rearrangement].

Uchida E, Watanabe K, Oshikawa G, Sakashita C, Kurosu T, Fukuda T, Arai A, Murakami N, Miura O, Yamamoto M.

Rinsho Ketsueki. 2016 Jan;57(1):47-51. doi: 10.11406/rinketsu.57.47. Review. Japanese.

PMID:
26861104
13.

Aneuploidy in Early Miscarriage and its Related Factors.

Jia CW, Wang L, Lan YL, Song R, Zhou LY, Yu L, Yang Y, Liang Y, Li Y, Ma YM, Wang SY.

Chin Med J (Engl). 2015 Oct 20;128(20):2772-6. doi: 10.4103/0366-6999.167352.

14.

[Trisomy 22 syndrome: a case report].

Yan JX, Liu XF, Wang GH, Yan CY.

Zhongguo Dang Dai Er Ke Za Zhi. 2015 Jul;17(7):753-4. Chinese. No abstract available.

PMID:
26182287
15.

[Trisomy 22 syndreom: a report of 2 cases].

He X, Yao D, Zhao ZY.

Zhongguo Dang Dai Er Ke Za Zhi. 2015 May;17(5):524-5. Chinese. No abstract available.

PMID:
26014708
16.

Severe psychomotor delay in a severe presentation of cat-eye syndrome.

Jedraszak G, Receveur A, Andrieux J, Mathieu-Dramard M, Copin H, Morin G.

Case Rep Genet. 2015;2015:943905. doi: 10.1155/2015/943905. Epub 2015 Jan 14.

17.

The typology and function of private speech in a young man with intellectual disabilities: An empirical case study.

Lechler S, Hare DJ.

J Intellect Disabil. 2015 Jun;19(2):149-58. doi: 10.1177/1744629514564449. Epub 2014 Dec 28.

PMID:
25548198
18.

Co-occurrence of non-mosaic trisomy 22 and inherited balanced t(4;6)(q33;q23.3) in a liveborn female: case report and review of the literature.

Kehinde FI, Anderson CE, McGowan JE, Jethva RN, Wahab MA, Glick AR, Sterner MR Jr, Pascasio JM, Punnett HH, Liu J.

Am J Med Genet A. 2014 Dec;164A(12):3187-93. doi: 10.1002/ajmg.a.36778. Epub 2014 Sep 24. Review.

PMID:
25257307
19.

Acute myeloid leukemia presenting as "bowel upset": a case report.

Gajendra S, Gogia A, Das P, Gupta R, Tanwar P.

J Clin Diagn Res. 2014 Jul;8(7):FD09-10. doi: 10.7860/JCDR/2014/9112.4578. Epub 2014 Jul 20.

20.

Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory.

Wang BT, Chong TP, Boyar FZ, Kopita KA, Ross LP, El-Naggar MM, Sahoo T, Wang JC, Hemmat M, Haddadin MH, Owen R, Anguiano AL.

Mol Cytogenet. 2014 May 22;7:33. doi: 10.1186/1755-8166-7-33. eCollection 2014.

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